FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FORCEP

K Number: K812205 · Decision Oct 26, 1981
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
9
Review Days
83

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Basic Information

Device Name
FORCEP
K Number
K812205
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Reznik Instruments
Date Received
August 4, 1981
Decision Date
October 26, 1981
Product Code
GEN
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEN Forceps, General & Plastic Surgery

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Other Clearances by Reznik Instruments

K Number Device Name
K812201 PHOTOGRAPHIC EQUIPMENT
K812203 ELECTROSURGICAL UNIT
K812206 LAPAROSCOPE
K812199 TROCAR & TROCAR SLEEVES
K812204 UTERINE MANIPULATORS
K812200 INSUFFLATOR
K812202 FIBER OPTIC LIGHT SOURCE
K812198 ACCESSORIES(PROBES, SUCTION TUBES, ETC.)